Novel targeting strategy based on multimeric ligands for drug delivery and molecular imaging: homooligomers of alpha-MSH

Bioorg Med Chem Lett. 2004 Jan 5;14(1):211-5. doi: 10.1016/j.bmcl.2003.09.079.


Homooligomers constructed with 4- and 6-amino acid fragments of melanocortin (alpha-MSH) bind with higher affinity and with apparent cooperativity to melanocortin receptor, compared to their constituent monomers. Individual ligands were tethered with various spacers of different length and rigidity and the influence of spacers on binding was studied. Binding assays were performed on cells transfected with the melanocortin receptor, hMC4R. There is a 5-7-fold decrease in the EC(50) with the addition of each subunit, going from monomer to trimer. The Hill coefficient increases from 0.76 for the monomer to 1.12 for the dimer and 1.35 for the trimer. These data show a general trend of increasing avidity with increasing number of ligands in oligomers.

Publication types

  • Research Support, U.S. Gov't, P.H.S.

MeSH terms

  • Cell Line
  • Dimerization
  • Dose-Response Relationship, Drug
  • Drug Delivery Systems / methods*
  • Humans
  • Ligands
  • Models, Molecular*
  • Protein Binding
  • alpha-MSH / chemistry*
  • alpha-MSH / metabolism*


  • Ligands
  • alpha-MSH